Canonical Allele Identifier: CA2066032950

Gene: NOS1

Linked Data

• dbSNP Id: rs1875997008

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117339510A>C , CM000674.2:g.117339510A>C	GRCh38
NC_000012.11:g.117777315A>C , CM000674.1:g.117777315A>C	GRCh37
NC_000012.10:g.116261698A>C	NCBI36
NG_011991.2:g.27268T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.-420-8021T>G MANE Select	ENSP00000320758.6:n.-420-8021T>G
ENST00000317775.10:c.-420-8021T>G	ENSP00000320758.6:n.-420-8021T>G
ENST00000549189.1:n.471-8021T>G
ENST00000618760.4:c.-420-8021T>G	ENSP00000477999.1:n.-420-8021T>G
NM_000620.4:c.-420-8021T>G	NP_000611.1:n.-420-8021T>G
NM_001204218.1:c.-420-8021T>G	NP_001191147.1:n.-420-8021T>G
XM_011538398.1:c.-420-8021T>G	XP_011536700.1:n.-420-8021T>G
NM_000620.5:c.-420-8021T>G MANE Select	NP_000611.1:n.-420-8021T>G
NM_001204218.2:c.-420-8021T>G	NP_001191147.1:n.-420-8021T>G